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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00698360
Other study ID # CREAM 1
Secondary ID R-07.03M
Status Completed
Phase N/A
First received June 13, 2008
Last updated June 16, 2008
Start date July 2007
Est. completion date June 2008

Study information

Verified date June 2008
Source Meander Medical Center
Contact n/a
Is FDA regulated No
Health authority Netherlands: Medical Ethics Review Committee (METC)
Study type Observational

Clinical Trial Summary

Rationale: Investigation of the circadian rhythm of erythropoietin and melatonin in patients with various degrees of renal insufficiency

Objectives:

Primary objective: Is there a circadian rhythm of epo and melatonin in patients with various degrees of renal insufficiency?

Primary Objective: Is there a circadian rhythm of epo and melatonin in patients with various degrees of renal insufficiency compared to patients with a normal renal function?

Secondary Objective: Is there a circadian rhythm of cortisol and IGF in patients with various degrees of renal insufficiency?

Secondary Objective: Is there a circadian rhythm of cortisol and IGF in patients with various degrees of renal insufficiency compared to patients with a normal renal function?

Study design: Comparative study in 4 groups with various degrees of renal insufficiency, duration for each patient 24 hrs. Total duration of study 12 months, patients admitted to the hospital (on nursing ward)

Study population: Patients with various degrees of renal insufficiency

Main study parameters/endpoints: Analysis of the existence of a circadian rhythm in patients with a normal renal function and in patients with variable degrees of renal insufficiency

Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Better knowledge of the circadian rhythm in renal insufficiency. This could lead to a more efficient administration of erythropoietin and melatonin in the future.

Extent of burden is 1 venapunction for placement of infusion needle, the withdrawal of 11 times 5 ml blood in 24 hrs, continuous measurement of body temperature via capsule, 24-hour continuous ambulant blood pressure monitoring.


Recruitment information / eligibility

Status Completed
Enrollment 34
Est. completion date June 2008
Est. primary completion date June 2008
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 85 Years
Eligibility Inclusion criteria:

- Patient with various degrees of renal insufficiency, stable creatinin clearance: minimum 10 ml/min (measured with MDRD), admitted to our hospital

- Informed Consent

- Man/Women between 18 and 85 years

- Understanding and knowledge of the dutch language

Exclusion criteria:

- Instable angina pectoris, heart failure NYHA class IV

- Therapy with erythropoetin, melatonin and hypnotics

- Acute renal failure or rapidly progressive glomerulonephritis

- Bleeding or hemolysis as a cause of anemia

- Deficiency of iron, folate and/or vitamin B12

- Presence of chronic inflammatory disease or clinically significant infection

- Hemoglobinopathies

- Alcohol and/or drug abuse

- Enrolment in another study

- Any kind of disorder that compromises the ability of the subject to give written informed consent and/or to comply with study procedures

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Locations

Country Name City State
Netherlands Meander Medical Center Amersfoort

Sponsors (3)

Lead Sponsor Collaborator
Meander Medical Center Hoffmann-La Roche, Stichting Bijstand, Meander Medical Center

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary existence of circadian rhythm of Erythropoietin and Melatonin 24 hours No
Secondary existence of a circadian rhythm of cortisol and IGF-1 24 hours No
Secondary Relationship between temperature and melatonin. Relationship between blood pressure and erythropoietin 24 hours No
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